Bids Are Invited For Acquisition Of Hospital Medical Material (Apron, Cannula, Wire Etc), To Compose The Price Registration System.

Canula, Endo-Tracheal, With Cuff N. 7, 0, Disposable, Sterile, In Pvc, Siliconized, Transparent, Atoxic, With High Volume And Low Pressure, Semi-Hot Connector, Opaque Cuff, Retracted Tip, Radiopaca Line Continues, Maglli Curve, Pilot And Valve Marks, Indicative Marks Of Depth By The Body Of The Body Cannula And Caliber Marked In A Cannula Location. Individual Inbailating, In Surgical Degree And Thermoplastic Film, Opening In Petala. In The Packaging Should Be Printed Identification Data, Procedure, Manufacturing Date, Type Of Sterilization, Expiration Date And Registration In The Ministry Of Health, With Cuff N. 8, 5, Wire, For Unique Use, Linen 2-0, 70 Cm Long (Can Vary In + Or - 5 Cm), Cylinder -Ended Needle, 3/8 Circle And 3 Cm In Length, For Closure And Surgeries Of The Digestive Tract. Packaging: Primary Packaging Packaged Individually According To Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Asptic, Sterile And Apirogenic Technique; Primary Packaging Must Contain Product Identification And Characteristics, Such As: Manufacturer Name, Lot, Product Validity, Sterilization Method, Sterilization Validity; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use; The Product Must Obey Any Legislation That Is Inherent In It. Rotulating: Primari Packaging, Probe, Tracheal Aspiration, N. 16, Malleable, Attractive, With 01 Distal Orifice, 02 On The Sides And Universal Connector. Primary Inbound In Accordance With Packaging Rules That Guarantee The Integrity Of The Product Until The Time Of Its Use, Allowing And Opening And Transfers With Asptic Technique; The Label Of The Primary Packaging And /Or The Product Itself Must Contain Information, Written In The Language In Portuguese: Name Of Manufacturer, Name And Mark Of The Product, Validity Period, Exposure, Validity Of Sterilization, Registration Number At Anvisa /Ms, Name Of The Responsible Technician; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use. Primary And Secondary Packaging Labeled According To The Current Legislation Of Anvisa. The Product Must Obey Q, Apron, (Cover), Not Sterile, Made Of Trilaminated Sms, For Hospital Medical Use, Waterproof Body And Liquid Fluids, Jammed, Hypoallergenic, Ergonomic, Closed Front With The Back, Front Strip, For Back Closure, Long Sleeves, Mesh Or Elastic, Knitted Handle 50 Gr/M² Minimum, Total Minimum Width 1, 50 Cm And Minimum Length Of 1, 25 Cm. Must Register At Anvisa/Ms. Individual, Primary And Secondary Packaging Labeled According To Rdc 185/01 Anvisa, The Product Must Obey Current Legislation.